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Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men
Methamphetamine (MA) use is a major public health problem in the United States, especially among people living with HIV (PLWH). Many MA-induced neurotoxic effects are mediated by inflammation and gut microbiota may play a role in this process, yet the effects of MA on the microbiome have not been ad...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795845/ https://www.ncbi.nlm.nih.gov/pubmed/31619731 http://dx.doi.org/10.1038/s41598-019-51142-8 |
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author | Cook, Ryan R. Fulcher, Jennifer A. Tobin, Nicole H. Li, Fan Lee, David J. Woodward, Cora Javanbakht, Marjan Brookmeyer, Ron Shoptaw, Steve Bolan, Robert Aldrovandi, Grace M. Gorbach, Pamina M. |
author_facet | Cook, Ryan R. Fulcher, Jennifer A. Tobin, Nicole H. Li, Fan Lee, David J. Woodward, Cora Javanbakht, Marjan Brookmeyer, Ron Shoptaw, Steve Bolan, Robert Aldrovandi, Grace M. Gorbach, Pamina M. |
author_sort | Cook, Ryan R. |
collection | PubMed |
description | Methamphetamine (MA) use is a major public health problem in the United States, especially among people living with HIV (PLWH). Many MA-induced neurotoxic effects are mediated by inflammation and gut microbiota may play a role in this process, yet the effects of MA on the microbiome have not been adequately explored. Therefore, we performed 16S rRNA gene sequencing on rectal swab samples from 381 men who have sex with men, 48% of whom were PLWH and 41% of whom used MA. We compared microbiome composition between MA users and non-users while testing for potential interactions with HIV and controlling for numerous confounders using inverse probability of treatment weighting. We found that MA use explained significant variation in overall composition (R(2) = 0.005, p = 0.008) and was associated with elevated Finegoldia, Parvimonas, Peptoniphilus, and Porphyromonas and reduced Butyricicoccus and Faecalibacterium, among others. Genera including Actinomyces and Streptobacillus interacted with HIV status, such that they were increased in HIV+ MA users. Finegoldia and Peptoniphilus increased with increasing frequency of MA use, among others. In summary, MA use was associated with a microbial imbalance favoring pro-inflammatory bacteria, including some with neuroactive potential and others that have previously been associated with poor HIV outcomes. |
format | Online Article Text |
id | pubmed-6795845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67958452019-10-25 Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men Cook, Ryan R. Fulcher, Jennifer A. Tobin, Nicole H. Li, Fan Lee, David J. Woodward, Cora Javanbakht, Marjan Brookmeyer, Ron Shoptaw, Steve Bolan, Robert Aldrovandi, Grace M. Gorbach, Pamina M. Sci Rep Article Methamphetamine (MA) use is a major public health problem in the United States, especially among people living with HIV (PLWH). Many MA-induced neurotoxic effects are mediated by inflammation and gut microbiota may play a role in this process, yet the effects of MA on the microbiome have not been adequately explored. Therefore, we performed 16S rRNA gene sequencing on rectal swab samples from 381 men who have sex with men, 48% of whom were PLWH and 41% of whom used MA. We compared microbiome composition between MA users and non-users while testing for potential interactions with HIV and controlling for numerous confounders using inverse probability of treatment weighting. We found that MA use explained significant variation in overall composition (R(2) = 0.005, p = 0.008) and was associated with elevated Finegoldia, Parvimonas, Peptoniphilus, and Porphyromonas and reduced Butyricicoccus and Faecalibacterium, among others. Genera including Actinomyces and Streptobacillus interacted with HIV status, such that they were increased in HIV+ MA users. Finegoldia and Peptoniphilus increased with increasing frequency of MA use, among others. In summary, MA use was associated with a microbial imbalance favoring pro-inflammatory bacteria, including some with neuroactive potential and others that have previously been associated with poor HIV outcomes. Nature Publishing Group UK 2019-10-16 /pmc/articles/PMC6795845/ /pubmed/31619731 http://dx.doi.org/10.1038/s41598-019-51142-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cook, Ryan R. Fulcher, Jennifer A. Tobin, Nicole H. Li, Fan Lee, David J. Woodward, Cora Javanbakht, Marjan Brookmeyer, Ron Shoptaw, Steve Bolan, Robert Aldrovandi, Grace M. Gorbach, Pamina M. Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men |
title | Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men |
title_full | Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men |
title_fullStr | Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men |
title_full_unstemmed | Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men |
title_short | Alterations to the Gastrointestinal Microbiome Associated with Methamphetamine Use among Young Men who have Sex with Men |
title_sort | alterations to the gastrointestinal microbiome associated with methamphetamine use among young men who have sex with men |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795845/ https://www.ncbi.nlm.nih.gov/pubmed/31619731 http://dx.doi.org/10.1038/s41598-019-51142-8 |
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